Canonical Allele Identifier: CA387755050

Gene: BRCA2

Linked Data

• ClinVar Variation Id: 836772
• ClinVar RCV Id: RCV001037970 ; RCV002445219
• dbSNP Id: rs2072876301
• MyVariant Identifiers: chr13:g.32950917G>A (hg19) ; chr13:g.32376780G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.32376780G>A , CM000675.2:g.32376780G>A	GRCh38
NC_000013.10:g.32950917G>A , CM000675.1:g.32950917G>A	GRCh37
NC_000013.9:g.31848917G>A	NCBI36
NG_012772.3:g.66301G>A , LRG_293:g.66301G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470094.2:c.8743G>A	ENSP00000434898.2:p.Ala2915Thr
ENST00000528762.2:c.*110G>A	ENSP00000433168.2:n.*110G>A
ENST00000530893.7:c.8374G>A	ENSP00000499438.2:p.Ala2792Thr
ENST00000665585.2:c.*305G>A	ENSP00000499570.2:n.*305G>A
ENST00000666593.2:c.8743G>A	ENSP00000499256.2:p.Ala2915Thr
ENST00000700202.2:c.8743G>A	ENSP00000514856.2:p.Ala2915Thr
ENST00000700202.1:c.1210G>A	ENSP00000514856.1:p.Ala404Thr
ENST00000700203.1:n.870G>A
ENST00000380152.8:c.8743G>A MANE Select	ENSP00000369497.3:p.Ala2915Thr
ENST00000544455.6:c.8743G>A	ENSP00000439902.1:p.Ala2915Thr
ENST00000614259.2:c.8751G>A	ENSP00000506251.1:n.8751G>A
ENST00000665585.1:c.1621G>A
ENST00000680887.1:c.8743G>A	ENSP00000505508.1:p.Ala2915Thr
ENST00000380152.7:c.8743G>A	ENSP00000369497.3:p.Ala2915Thr
ENST00000528762.1:c.305G>A	ENSP00000433168.1:n.305G>A
ENST00000544455.5:c.8743G>A	ENSP00000439902.1:p.Ala2915Thr
NM_000059.3:c.8743G>A , LRG_293t1:c.8743G>A	NP_000050.2:p.Ala2915Thr
XM_011535203.1:c.8743G>A	XP_011533505.1:p.Ala2915Thr
XM_011535204.1:c.8647G>A	XP_011533506.1:p.Ala2883Thr
XM_011535205.1:c.8743G>A	XP_011533507.1:p.Ala2915Thr
NM_000059.4:c.8743G>A MANE Select	NP_000050.3:p.Ala2915Thr